QA/CSV Validation Analyst - GxP, MyLabData , Windows 11, Empower - Hybrid, Greater London
Posted 1 day ago by MRP-Global
Negotiable
Undetermined
Hybrid
Greater London, England, United Kingdom
Summary: A global organization is seeking a QA/CSV Validation Analyst to support the implementation of My Lab data, Windows 11, and Empower. This role is a contract position lasting 6-12 months with potential for extensions, requiring a hybrid working arrangement of 2-3 days onsite in Greater London. The ideal candidate will have expertise in CSV and equipment validation, along with experience in regulated environments.
Key Responsibilities:
- CSV and equipment validation expertise.
- Strong understanding of laboratory record keeping, data integrity, and software validation principles.
- Familiarity with electronic laboratory notebook systems, audit trail functionality, and validation of computerized systems.
- Quality experiences.
- Analytical and critical thinking.
- Collaboration and teamwork.
- Document review and approval processes in line with GxP and regulatory requirements.
Key Skills:
- At least 3 years’ experience in a laboratory, quality assurance, or data management role within a regulated environment.
- Experience in pharmaceuticals, biotechnology, or clinical research.
- Demonstrable experience with document review and approval processes.
Salary (Rate): undetermined
City: Greater London
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
A large global organisation are looking for a QA/CSV Validation Analyst to assist on an implementation of My Lab data, Windows 11 and Empower. This will be an initial 6-12 months+ contract with the opportunity for multiple extensions. The role will be worked on a hybrid basis, 2/3 days a week onsite in Greater London.
Key Responsibilities/Skills:
- CSV and equipment validation expertise: Strong understanding of laboratory record keeping, data integrity, and software validation principles.
- Familiarity with electronic laboratory notebook systems, audit trail functionality, and validation of computerised systems (e.g., Windows 11 environments).
- Quality experiences
- Analytical and critical thinking
- Collaboration and teamwork
- At least 3 years’ experience in a laboratory, quality assurance, or data management role within a regulated environment (such as pharmaceuticals, biotechnology, or clinical research).
- Demonstrable experience with document review and approval processes, preferably in line with GxP and regulatory requirements.